Marchantia berteroana - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Marchantia berteroana - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID64405139574f1111096473
Scientific name Marchantia berteroana
Authority Lehm. & Lindenb.
First published in Nov. Stirp. Pug. 6: 21 1834

Description Top

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Marchantia berteroana is a species of liverwort that belongs to the genus Marchantia. It has a flat, thalloid body with a glossy surface and can range in color from dark green to yellow. The plant reproduces both sexually and asexually, with male and female gametangia growing vertically from the thallus. It also contains flavones that change in composition and amount depending on the reproductive state of the plant. This species can be distinguished from similar species, such as Marchantia polymorpha, by its brighter green color and transparent scales on the underside of the thallus. It can be found in various locations around the world, including Australia, New Zealand, and Antarctica, and prefers moist environments. It is also known to be one of the first species to colonize after a bushfire in Tasmanian mixed forests.

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No known synonyms.

Common names Top

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Language Common/alternative name
Arabic كبدية لوحية

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Varieties (abbr. var.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001203244
Tropicos 35202683
INPN 657316
The Plant List tro-35202683
Open Tree Of Life 3856100
NCBI Taxonomy 2078533
iNaturalist 327478
GBIF 2688572
Freebase /m/0t_dm0f
EOL 6076196
Wikipedia Marchantia_berteroana

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Can vegetation be discretely classified in species‐poor environments? Testing plant community concepts for vegetation monitoring on sub‐Antarctic Marion Island van der Merwe S, Greve M, Skowno AL, Hoffman MT, Cramer MD Ecol Evol 03-Jan-2023
PMCID:PMC9811060
doi:10.1002/ece3.9681
PMID:36620413
Metabolite profiling reveals organ‐specific flavone accumulation in Scutellaria and identifies a scutellarin isomer isoscutellarein 8‐O‐β‐glucuronopyranoside Askey BC, Liu D, Rubin GM, Kunik AR, Song YH, Ding Y, Kim J Plant Direct 20-Dec-2021
PMCID:PMC8689113
doi:10.1002/pld3.372
PMID:34977451
It Is Hot in the Sun: Antarctic Mosses Have High Temperature Optima for Photosynthesis Despite Cold Climate Perera-Castro AV, Waterman MJ, Turnbull JD, Ashcroft MB, McKinley E, Watling JR, Bramley-Alves J, Casanova-Katny A, Zuniga G, Flexas J, Robinson SA Front Plant Sci 07-Aug-2020
PMCID:PMC7457050
doi:10.3389/fpls.2020.01178
PMID:32922412
The distribution and evolution of fungal symbioses in ancient lineages of land plants Rimington WR, Duckett JG, Field KJ, Bidartondo MI, Pressel S Mycorrhiza 04-Mar-2020
PMCID:PMC7062687
doi:10.1007/s00572-020-00938-y
PMID:32130512
Evolution and networks in ancient and widespread symbioses between Mucoromycotina and liverworts Rimington WR, Pressel S, Duckett JG, Field KJ, Bidartondo MI Mycorrhiza 13-Nov-2019
PMCID:PMC6890582
doi:10.1007/s00572-019-00918-x
PMID:31720838
Field Guide to Plant Model Systems Chang C, Bowman JL, Meyerowitz EM Cell 06-Oct-2016
PMCID:PMC5068971
doi:10.1016/j.cell.2016.08.031
PMID:27716506
Isoscutellarein and hypolaetin 8-glucuronides from the liverwort Marchantia berteroana Kenneth R. Markham, Lawrence J. Porter Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(75)85194-6
Biosynthesis of cyclic bis(bibenzyls) in Marchantia polymorpha Susanne Friederich, Ulrich H Maier, Brigitte Deus-Neumann, Yoshinori Asakawa, Meinhart H. Zenk Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00557-3

Phytochemical Profile Top

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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
2-Methyl-5-(1,2,2-trimethylcyclopentyl)phenol 586002 Click to see CC1=C(C=C(C=C1)C2(CCCC2(C)C)C)O 218.33 unknown https://doi.org/10.1016/S0031-9422(98)00557-3
Phenol, 2-methyl-5-(1,2,2-trimethylcyclopentyl)-, (S)- 11790670 Click to see CC1=C(C=C(C=C1)C2(CCCC2(C)C)C)O 218.33 unknown https://doi.org/10.1016/S0031-9422(98)00557-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-8-O-glucuronides
(2R,3R,4S,5S,6R)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-8-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 162945496 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1016/0031-9422(75)85194-6
(2R,3R,4S,5S,6R)-6-[4-[8-[(2R,3S,4S,5R,6R)-6-carboxy-3,4,5-trihydroxyoxan-2-yl]oxy-5,7-dihydroxy-4-oxochromen-2-yl]-2-hydroxyphenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 162880421 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)OC5C(C(C(C(O5)C(=O)O)O)O)O 654.50 unknown https://doi.org/10.1016/0031-9422(75)85194-6
6-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-8-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 14887604 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1016/0031-9422(75)85194-6
6-[4-[8-(6-Carboxy-3,4,5-trihydroxyoxan-2-yl)oxy-5,7-dihydroxy-4-oxochromen-2-yl]-2-hydroxyphenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 74977920 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)OC5C(C(C(C(O5)C(=O)O)O)O)O 654.50 unknown https://doi.org/10.1016/0031-9422(75)85194-6

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